Page B D, Kennedy B P
J Assoc Off Anal Chem. 1975 Sep;58(5):1062-8.
A quantitative gas chromatographic (GC) method is described for the determination of residual methylene chloride, ethylene dichloride, and trichloroethylene in spice oleoresins. The proposed method involves vacuum distillation in a closed system with toluene as a carrier solvent. Quantitation by electron capture GC on Porapak Q is facilitated by water extraction and by the addition of trans-1,2-dichloroethylene as an internal standard. Recoveries from oleoresins spiked at 30, 15, and 6 ppm ranged from 93 to 102%. To assess the possibility of interference from spice volatiles, the procedure was applied to 17 different spice oleoresins from 3 different manufacturers. No interferences were found, but methylene chloride levels up to 83 ppm and ethylene dichloride levels up to 23 ppm were detected. Trichloroethylene was not detected in any of the oleoresins.
描述了一种定量气相色谱(GC)方法,用于测定香料油树脂中残留的二氯甲烷、二氯乙烯和三氯乙烯。所提出的方法涉及在封闭系统中以甲苯作为载溶剂进行减压蒸馏。通过水萃取并添加反式-1,2-二氯乙烯作为内标,便于在Porapak Q上通过电子捕获气相色谱进行定量分析。在添加浓度为30、15和6 ppm的油树脂中的回收率为93%至102%。为评估香料挥发物干扰的可能性,该程序应用于来自3个不同制造商的17种不同的香料油树脂。未发现干扰,但检测到二氯甲烷含量高达83 ppm,二氯乙烯含量高达23 ppm。在任何一种油树脂中均未检测到三氯乙烯。